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胼胝体发育不全与垂体功能减退。

Dysgenesis of the corpus callosum and hypopituitarism.

作者信息

Smith P J, Hindmarsh P, Kendall B, Brook C G

出版信息

Acta Paediatr Scand. 1986 Nov;75(6):923-6. doi: 10.1111/j.1651-2227.1986.tb10318.x.

Abstract

A high resolution CT scan demonstrated the unexpected finding of dysgenesis of the corpus callosum in addition to the expected finding of pituitary hypoplasia in three children who presented with growth failure secondary to hypopituitarism. Several of the clinical features reported in association with dysgenesis of the corpus callosum may be ascribed to hypothalamo-pituitary dysfunction. These children emphasize the need to assess the endocrine function of patients with midline structural defects. It should not be assumed that the clinical manifestations are related solely to the anatomical abnormality.

摘要

高分辨率CT扫描显示,在三名因垂体功能减退继发生长发育迟缓的儿童中,除了预期的垂体发育不全外,还意外发现了胼胝体发育不全。与胼胝体发育不全相关的一些临床特征可能归因于下丘脑 - 垂体功能障碍。这些儿童强调了评估中线结构缺陷患者内分泌功能的必要性。不应假定临床表现仅与解剖学异常有关。

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